Immunological studies of aging. II. Loss of IgG and high avidity plaque-forming cells and increased suppressor cell activity in aging mice
- PMID: 62009
- PMCID: PMC2190420
- DOI: 10.1084/jem.144.4.1037
Immunological studies of aging. II. Loss of IgG and high avidity plaque-forming cells and increased suppressor cell activity in aging mice
Abstract
The magnitude and heterogeneity of the immune response to dinitrophenylated bovine gamma globulin was measured in aged and young mice at a cellular level using an inhibition of plaque-forming cell assay. The primary and secondary responses of 24-mo-old mice were markedly depressed in magnitude and restricted in avidity for the DNP determinant when compared to 2-mo-old animals. Bacterial lipopolysaccharide given at the time of immunization increased the restriction in heterogeneity seen in 12- and 24-mo-old mice. Indirect PFCs were more severely depressed than direct PFCs in 24-mo-old mice. Syngeneic, lethally irradiated, 2-mo-old mice reconstituted with aged spleen cells exhibit the depressed and restricted response to DNP-BGG seen in old mice. When 10(8) young thymus cells were given together with old spleen cells the heterogeneity of the response was increased. When 2-mo- and 24-mo-old spleen cells were transferred together into young recipients the magnitude of the response to the young spleen cells markedly reduced. Thus, there appears to be a loss of thymic-helper cells and an increase in suppressor activity in aged animals.
Similar articles
-
Old mice recover the ability to produce IgG and high-avidity antibody following irradiation with partial bone marrow shielding.Proc Natl Acad Sci U S A. 1988 Feb;85(4):1169-73. doi: 10.1073/pnas.85.4.1169. Proc Natl Acad Sci U S A. 1988. PMID: 3257573 Free PMC article.
-
Immunological studies of aging. IV. The contribution of thymic involution to the immune deficiencies of aging mice and reversal with thymopoietin32-36.J Exp Med. 1978 Oct 1;148(4):996-1006. doi: 10.1084/jem.148.4.996. J Exp Med. 1978. PMID: 81262 Free PMC article.
-
Differential effect of aging on the heterogeneity of the immune response to a T-dependent antigen in systemic and mucosal-associated lymphoid tissues.J Immunol. 1981 Feb;126(2):472-7. J Immunol. 1981. PMID: 7005339
-
Isolation of antigen-binding cells from unprimed mice: demonstration of antibody-forming cell precursor activity and correlation between precursor and secreted antibody avidities.J Exp Med. 1974 Oct 1;140(4):904-20. doi: 10.1084/jem.140.4.904. J Exp Med. 1974. PMID: 4139227 Free PMC article.
-
Aging. Polymorphism, compartmentalization and environmental impact.Immunol Lett. 1994 Jun;40(3):213-7. doi: 10.1016/0165-2478(94)00058-1. Immunol Lett. 1994. PMID: 7525463 Review.
Cited by
-
Aging impairs murine B cell differentiation and function in primary and secondary lymphoid tissues.Aging Dis. 2011 Oct;2(5):361-73. Epub 2011 Oct 28. Aging Dis. 2011. PMID: 22396888 Free PMC article.
-
Age-dependent variations of antibody avidity.Immunology. 1978 Oct;35(4):601-11. Immunology. 1978. PMID: 361545 Free PMC article.
-
The effect of age on the B-cell repertoire.J Clin Immunol. 2000 Jul;20(4):240-9. doi: 10.1023/a:1006659401385. J Clin Immunol. 2000. PMID: 10939711 Review.
-
CD4 T cell memory derived from young naive cells functions well into old age, but memory generated from aged naive cells functions poorly.Proc Natl Acad Sci U S A. 2003 Dec 9;100(25):15053-8. doi: 10.1073/pnas.2433717100. Epub 2003 Dec 1. Proc Natl Acad Sci U S A. 2003. PMID: 14657384 Free PMC article.
-
Effect of age on the induction of autoantibodies.Clin Exp Immunol. 1981 Apr;44(1):24-30. Clin Exp Immunol. 1981. PMID: 7021024 Free PMC article.